Evidence map›Paper›PMID 27536098›Full record

ArticleInternational journal of nanomedicine2016

Size-dependent cytotoxicity of Fe3O4 nanoparticles induced by biphasic regulation of oxidative stress in different human hepatoma cells.

Yuexia Xie, Dejun Liu, Chenlei Cai, Xiaojing Chen, Yan Zhou, Liangliang Wu, Yongwei Sun, Huili Dai, Xianming Kong, Peifeng Liu

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.6field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 73 citations in OpenAlex.

  1. Green synthesis of ZnO/FeRSC advances · 2026
    Article
  2. In Vitro Antitumor Effects of Melittin Attached to FeMolecules (Basel, Switzerland) · 2026
    Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Anticancer Effects of ZnO/CNT@FeInternational journal of hematology-oncology and stem cell research · 2022
    Article
  13. Article
  14. Thiolation of Myco-Synthesized FeJournal of fungi (Basel, Switzerland) · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Yuexia XieCentral Laboratory; State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute.
Dejun LiuDepartment of Biliary-Pancreatic Surgery, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, People's Republic of China.
Chenlei CaiCentral Laboratory.
Xiaojing ChenCentral Laboratory.
Yan ZhouCentral Laboratory.
Liangliang WuCentral Laboratory.
Yongwei SunDepartment of Biliary-Pancreatic Surgery, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, People's Republic of China.
Huili DaiCentral Laboratory; State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute.
Xianming KongCentral Laboratory; State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute.
Peifeng LiuCentral Laboratory; State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute.
Renji Hospital · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The application of Fe3O4 nanoparticles (NPs) has made great progress in the diagnosis of disease and in the drug delivery system for cancer therapy, but the relative mechanisms of potential toxicity induced by Fe3O4 have not kept pace with its development in the application, which has hampered its further clinical application. In this article, we used two kinds of human hepatoma cell lines, SK-Hep-1 and Hep3B, to investigate the cytotoxic effects and the involved mechanisms of small Fe3O4 NPs with different diameters (6 nm, 9 nm, and 14 nm). Results showed that the size of NPs effectively influences the cytotoxicity of hepatoma cells: 6 nm Fe3O4 NPs exhibited negligible cytotoxicity and 9 nm Fe3O4 NPs affected cytotoxicity via cellular mitochondrial dysfunction and by inducing necrosis mediated through the mitochondria-dependent intracellular reactive oxygen species generation. Meanwhile, 14 nm Fe3O4 NPs induced cytotoxicity by impairing the integrity of plasma membrane and promoting massive lactate dehydrogenase leakage. These results explain the detailed mechanism of different diameters of small Fe3O4 NPs-induced cytotoxicity. We anticipate that this study will provide different insights into the cytotoxicity mechanism of Fe3O4 NPs, so as to make them safer to use in clinical application.

Indexed as

Magnetite NanoparticlesCarcinoma, HepatocellularCell Line, TumorCell MembraneHumansLiver NeoplasmsL-Lactate DehydrogenaseMitochondriaOxidative StressParticle SizeReactive Oxygen SpeciesL-Lactate DehydrogenaseMagnetite NanoparticlesReactive Oxygen Speciescytotoxicityhepatoma cellsmechanismnanoparticlesoxidative stress

Identifiers

PMID27536098
PMCPMC4973727
OpenAlexW2481258638

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.